UNKNOWN STEM Adverse Event — Injury (MDR 0001822565-2020-01477)
UNKNOWN STEM Adverse Event — Injury (MDR 0001822565-2020-01477) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN STEM; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER BIOMET, INC..
| Device | UNKNOWN STEM |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001822565-2020-01477 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | (B)(4). EVENT DATE (B)(6) 2020. EXPLANT DATE (B)(6) 2020. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION PROVIDED BY THE CUSTOMER. DHR WAS UNABLE TO BE REVIEWED AS THE LOT NUMBER FOR THE DEVICE IS UNKNOWN. THE ROOT CAUSE IS UNABLE TO BE DETERMINED. |
| Source | openFDA MAUDE (device adverse events) |
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